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在皱叶欧芹真菌感染部位质体ω-3脂肪酸去饱和酶mRNA的快速、短暂且高度局部化诱导。

Rapid, transient, and highly localized induction of plastidial omega-3 fatty acid desaturase mRNA at fungal infection sites in Petroselinum crispum.

作者信息

Kirsch C, Takamiya-Wik M, Reinold S, Hahlbrock K, Somssich I E

机构信息

Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Cologne, Germany.

出版信息

Proc Natl Acad Sci U S A. 1997 Mar 4;94(5):2079-84. doi: 10.1073/pnas.94.5.2079.

Abstract

Parsley (Petroselinum crispum) plants and suspension-cultured cells have been used extensively for studies of non-host-resistance mechanisms in plant/pathogen interactions. We now show that treatment of cultured parsley cells with a defined peptide elicitor of fungal origin causes rapid and large changes in the levels of various unsaturated fatty acids. While linoleic acid decreased and linolenic acid increased steadily for several hours, comparatively sharp increases in oleic acid followed a biphasic time course. In contrast, the overall level of stearic acid remained unaffected. Using a PCR-based approach, a parsley cDNA was isolated sharing high sequence similarity with omega-3 fatty acid desaturases. Subsequent isolation and characterization of a full-length cDNA enabled its functional identification as a plastid-localized omega-3 fatty acid desaturase by complementation of the Arabidopsis thaliana fad7/8 double mutant which is low in trienoic fatty acids. omega-3 Fatty acid desaturase mRNA accumulated rapidly and transiently in elicitor-treated cultured parsley cells, protoplasts, and leaves, as well as highly localized around fungal infection sites in parsley leaf buds. These results indicate that unsaturated fatty acid metabolism is yet another component of the highly complex, transcriptionally regulated pathogen defense response in plants.

摘要

欧芹(Petroselinum crispum)植株和悬浮培养细胞已被广泛用于植物/病原体相互作用中非宿主抗性机制的研究。我们现在表明,用一种特定的真菌来源的肽激发子处理培养的欧芹细胞会导致各种不饱和脂肪酸水平迅速发生巨大变化。在几个小时内,亚油酸减少而亚麻酸稳步增加,相比之下,油酸的相对急剧增加呈现双相时间进程。相反,硬脂酸的总体水平未受影响。采用基于聚合酶链反应(PCR)的方法,分离出一个与ω-3脂肪酸去饱和酶具有高度序列相似性的欧芹互补DNA(cDNA)。随后对全长cDNA的分离和表征通过对三烯脂肪酸含量低的拟南芥fad7/8双突变体进行互补,实现了其作为质体定位的ω-3脂肪酸去饱和酶的功能鉴定。ω-3脂肪酸去饱和酶信使核糖核酸(mRNA)在激发子处理的培养欧芹细胞、原生质体和叶片中迅速且短暂地积累,并且在欧芹叶芽的真菌感染部位高度局部化。这些结果表明,不饱和脂肪酸代谢是植物中高度复杂的、转录调控的病原体防御反应的另一个组成部分。

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